As espumas de polietileno são amplamente utilizadas. Suas aplicações vão de aparelhos domésticos a artefatos médicos, incluindo aplicações nas indústrias de construção civil e automobilística. As propriedades das espumas dependem da densidade e da sua estrutura celular, em outras palavras, da quantidade de células abertas e fechadas, da distribuição e do tamanho das células. Os métodos de produção de espumas de polietileno reticulado são classificados em dois tipos, de acordo com o método de reticulação. Um dos métodos é a reticulação química, que utiliza peróxidos como agente reticulante, O outro método é a reticulação por irradiação, utilizando feixe de elétrons. As espumas obtidas a partir do polietileno reticulado pelo processo de irradiação apresentam superfície lisa e homogênea, e são formadas basicamente por células fechadas. O objetivo deste trabalho foi utilizar a radiação ionizante para a formação de ligações cruzadas entre as moléculas de polietileno de baixa densidade (LDPE), que permitiu a obtenção das espumas. As suas propriedades mecânicas, térmicas e morfológicas foram avaliadas. As amostras de polietileno com densidade de 0,946 g/cm3, contendo 5% de azodicarbonamida (ADCA), agente expansor, foram irradiadas com feixe de elétrons de alta energia com doses de radiação de 10, 20, 30, 40, 50, 60, 80 e 100 kGy. Após a irradiação, as amostras de LDPE foram colocadas em um forno para expansão térmica e formação das espumas. Foi determinado o grau de reticulação das espumas. Algumas amostras também foram envelhecidas termicamente. O desempenho mecânico das amostras de espumas foi avaliado por meio de ensaios de tração e deformação, dureza, deformação permanente por compressão e resiliência. Também foram realizados ensaios de termogravimetria (TGA) e de microscopia eletrônica de varredura (MEV). Os resultados mostraram que no intervalo de doses de radiação estudadas, a resistência à tração aumenta com o aumento do grau de reticulação. Nos ensaios de resistência à compressão, a partir da dose de radiação de 40 kGy, observou-se um decréscimo nos valores obtidos. Já a resiliência sofreu pouca aheração. De acordo com a análise morfológica pode-se concluir que a dose de radiação de 30 kGy foi a que promoveu a formação de espumas com estrutura celular fechada e mais homogênea. / The polyethylene foams are widely used. Their main applications are used for both home appliances to medical equipments. Beside that, they have applications in building and automotive industries. The foam properties depend on the density and its cellular structure, that is, the amount of open and closed cells, of the distribution and size of them. The methods of the crosslinking polyethylene foam production are classified in two types, according to the crosslinking method. One method is based on the chemical crosslinking, which utilizes peroxide as crosslinking agent. In the other method, the crosslinking is induced by electron beam radiation. The foams obtained from the crosslinking polyethylene by irradiation process presented a smooth and the homogeneous surface, and are formed basically by closed cells. The aim of this study was to apply the ionizing radiation from electron beam to crosslink low density polyethylene (LDPE), to obtain foams. Their morphological, thermal and mechanical properties were studied to evaluate the obtained samples. The samples of low density polyethylene (0,946 g/cm3), containing 5% of azodicarbonamide (ADCA), as expander agent, were irradiated with electron beam with doses of 10, 20, 30, 40, 50, 60, 80 and 100 kGy. After the irradiation, these LDPE samples were put into an oven to obtain the foams. It was determined the crosslinking degree of the foams. Some samples were also thermically aged. The mechanical performance of the foams samples was evaluated by means of the tensile strenght, compression, hardness, permanent deformation by compression and resilience. It was also carried out thermogravimetry and scanning electron microscopy (SEM). The results have shown that, in the interval of radiation doses studied, that the tensile strength increases with the increase of the crosslinking degree. The compression resistance results obtained from with samples with to radiation dose of 40 kGy showed significant decreasing. The resilience measurements have shown only little variations. According to the morphological analysis it can be concluded that foams with radiation dose of 30 kGy have closed cellular structure more homogeneous and smooth morphology.

Les nouvelles technologies sont de plus en plus demandeuses de sources de forte densité d’énergie respectueuses de l’environnement. Les accumulateurs lithium-ion semblent être la meilleure solution pour les applications mobiles et pour le domaine de l’automobile. Afin de répondre aux besoins en énergie de plus en plus importants, de nouveaux matériaux d’électrode négative sont nécessaires pour remplacer le carbone qui a désormais atteint son stade de maturité. En particulier, les composites silicium/carbone (Si/C) semblent être prometteurs pour augmenter la densité d’énergie des accumulateurs mais présentent de faibles rétentions de capacité au cours du cyclage. L’amélioration de la cyclabilité des composites Si/C fait l’objet de ce travail de thèse. La synthèse des composites par atomisation avec de l’alcool polyvinylique comme précurseur carboné suivie d’une pyrolyse est présentée. Les performances électrochimiques des matériaux résultants sont comparées à celles obtenues par d’autres composites, élaborés par lyophilisation et par broyage. Les propriétés intrinsèques des composites ont été modifiées par deux voies différentes afin d’améliorer leur cyclabilité. Dans un premiers temps, les effets de la réticulation de l’alcool polyvinylique ont été étudiés, puis ceux liés à l’ajout d’un catalyseur favorisant la graphitisation du carbone. La cyclabilité des composites Si/C peut également être améliorée en modifiant la nature du liant utilisé lors de la préparation des électrodes. L’intérêt bénéfique de l’emploi de l’acide polyacrylique en remplacement du fluorure de polyvinylidène couramment utilisé dans des électrodes à base de composites Si/C est démontré. / New technologies require more and more environment friendly sources of high energy density. Lithium-ion batteries seem to be the best solution for mobile and automotive applications. In order to meet the future energy requirements, new negative electrode materials are needed to replace carbon which has now reached a mature stage. Especially, silicon/carbon composites (Si/C) appear to be promising candidates to increase the energy density of batteries, but they still present poor capacity retention upon cycling. The improvement of Si/C composites cyclability is the subject of this thesis. The synthesis of Si/C composites by spray drying with polyvinyl alcohol as carbon precursor, followed by pyrolysis, is presented. The electrochemical performances are compared with those obtained for other composites, prepared by freeze drying and ball-milling. The intrinsic properties of the composites were modified in two different ways to improve their cyclability. First, we studied the effects of polyvinyl alcohol crosslinking, and then those related to the graphitization of carbon contained in these composites. The cyclability of Si/C composites can also be improved by changing the nature of the binder used during the electrodes preparation. The beneficial interest of using polyacrylic acid in replacement of polyvinylidene fluoride binder commonly used in Si/C based electrodes is shown.

Orientador: Josimeri Hebling / Resumo: Objetivo: Avaliar a estabilidade mecânica e a atividade proteolítica de interfaces produzidas pela apliação de um adesivo convencional simplificado sobre a dentina biomodificada e seca. Métodos: Superfícies planas de dentina coronária foram criadas em 64 molares hígidos. Os dentes foram divididos em 4 grupos de acordo com a solução aplicada sobre a dentina condicionada: extrato de semente de uva 5% (GSE), glutaraldeído 5% (GD), Gluma Desensitizer ou água (controle). As soluções foram aplicadas por 60s seguido de lavagem e secagem com papel absorvente. Os dentes foram então subdivididos em dois grupos, nos quais a dentina condicionada foi mantida úmida ou foi seca com ar por 60s. O adesivo Optibond foi aplicado e em seguida foi construído um cilindro de resina. Decorridas 24h, os dentes foram cortados em espécimes (0,81 mm2 ), submetidos ao ensaio de microtração imediatamente ou após 12 meses de envelhecimento. Os mesmos procedimentos adesivos foram realizados em 32 dentes adicionais. Esses dentes foram seccionados em fatias de 0,5 mm de espessura, preparadas para os ensaios de nanoinfiltração e zimografia in situ (EnzChek). Os dados de resistência de união foram submetidos aos testes de ANOVA e Tukey (p<0,05), e os ensaios de nanoinfiltração e zimografia in situ foram apresentados descritivamente. Resultados: Redução significante da resistência de união imediata (ca. 65%) e aumento da atividade proteolítica e nanoilfiltração foi observado em interfaces produzidas sobre a dent... (Resumo completo, clicar acesso eletrônico abaixo) / Abstract: Objective: To evaluate the mechanical stability and the proteolytic activity of bonds created by a one-step, etch-and-rinse adhesive applied to cross-linked and air-dried etched dentin. Methods: Flat coronal dentin surfaces were produced in 64 sound molars. The teeth were divided into 4 groups according to the solution applied on the etched dentin: 5% grape seed extract, 5% glutaraldehyde, Gluma Desensitizer or deionized water (control). Solutions were applied for 60s followed by rinse and blot drying. Then, the teeth were separated into two subgroups: the etched dentin was kept moist or air dried for 60s. Optibond was applied followed by a composite resin buildup. After 24h, the teeth were cut into beams (0.81 mm²) which were microtensile tested immediately or after 12mo of storage. Additional teeth (n=32) were bonded as described and cut into 0.5 mm-thick slabs. The slabs were prepared for nanoleakage and in situ zymography analyses (EnzChek). Bond strength data were submitted to ANOVA and Tukey tests (p<0.05) while nanoleakage and zymography data were descriptively reported. Results: Significant reduction in bond strength (ca. 65%) and increase of the proteolytic activity was seen when the etched dentin was air-dried without previous biomodification. Conversely, bond strengths did not differ from those produced on wet dentin when collagen was cross-linked before air-drying, irrespective of the solution. For both moist and air-dried etched dentin, collagen cross-linking res... (Complete abstract click electronic access below) / Mestre

A challenging application space exists for high-aspect-ratio, high-fidelity dielectrics in micro-electro-mechanical system (MEMS), microelectronic, and photonic applications. Photosensitive polymers are widely used in these fields because they are relatively easy to process and pattern, and have good mechanical properties. Photosensitive polynorbornene (PNB)-based dielectrics have been shown to have high sensitivity, excellent photodefinition properties, and high mechanical strength making them suitable for MEMS, microelectronic packaging, and photonic applications. PNB-based dielectrics can be functionalized with epoxide, carboxylic acid, or fluorinated alcohol groups. Epoxy or carboxylic acid groups can be used to provide cross-linkable sites, resulting in improved chemical and thermal properties while fluorinated alcohol groups can provide solubility in aqueous base. The focus of this study has been on the epoxy-based cross-linking of ultraviolet and electron beam (e-beam) sensitive negative-tone PNB-based dielectrics. The impact of multifunctional epoxy-based additives on the cross-linking, photolithographic properties, and adhesion properties of the photosensitive PNB dielectric was investigated. High aspect ratio features of 13:1 (height:width) were produced in 40 µm thick films (a single coat) with straight side-wall profiles and high fidelity. Contrast values as high as 33.4 were obtained at doses below 15 mJ/cm2. To evaluate the polymer's suitability to MEMS and microelectronics applications, epoxy cross-linking reactions were studied as a function of processing condition through Fourier transform infrared spectroscopy (FTIR), nanoindentation, swelling and dielectric measurements. The fully cross-linked films had an elastic modulus of 2.9 GPa and hardness of 0.18 GPa which can improve the mechanical compliance of the packaging device. To explore the feasibility of the PNB dielectric as a highly sensitive e-beam resist for nano scale fabrication, the e-beam initiated reaction between PNB cross-linking sites and the multifunctional epoxy cross-linkers was investigated. In this study, the interaction of an e-beam with the PNB mixture and its compounds was investigated. The contrast, photodefinability, and e-beam activation of the components in the PNB formulations were studied. The PNB polymer had very high e-beam sensitivity and contrast. It was shown that the addition of a photoacid generator (PAG) to the polymer-epoxy mixture enhanced the contrast and sensitivity. Formulations with the additional cross-linker showed improved contrast, sensitivity, and substrate adhesion. 100 nm structures with 13.5 nm line edge roughness (LER) were fabricated. The influence of the developing time, the developer concentration, PEB, and film thickness on the contrast and sensitivity were studied. Structures with contrast values as high as approximately 8 were fabricated at doses as low as 0.38 µC/cm2. The acid-catalyzed epoxy ring opening reaction of the PNB dielectric was studied using FTIR spectroscopy. The photo and thermal acid generation initiated epoxy ring opening reactions and subsequent cross-linking of polymer. Additionally, polymer properties were characterized as a function of processing conditions for this polymer system. It was shown that thermal cure conditions have a substantial impact on the mechanical and electrical properties of the polymer. The rate and ultimate conversion of the epoxy ring opening reaction increased with increasing cure temperature, resulting in a higher degree of cross-linking at cure temperatures above 140°C. Degradation reactions occurred at temperatures above 160°C, indicating loss of epoxide cross-linking groups and linkages. These hypotheses were supported by electrical and mechanical property studies. It was shown that curing the PNB polymer at 160°C for 1 h after develop resulted in full epoxy ring opening and highest cross-link density. This sample showed lower dielectric constant (3.9), residual stress (20 MPa), and solvent swelling (3.1%). Variable frequency microwave (VFM) processing of the PNB dielectric was studied to investigate the rapid curing of the polymer at lower temperatures. The FTIR results showed that the microwave reaction rates were higher at each isothermal cure temperature compared to convective heating, indicating that the rapid VFM curing of PNB at low temperatures is feasible. The PNB film was fully cross-linked after 15 min VFM cure at the low temperature of 150˚C. The shortest time to fully cure the polymer was found to be 5 min at 160°C. Also, the feasibility of rapid VFM curing of PNB in air was studied. All samples VFM-cured (140˚C-180˚C) in air showed no signs of oxidation. The electrical and mechanical properties of VFM-cured films were characterized and compared with thermally cured films to determine the effectiveness of the VFM processing. VFM-cured samples showed higher degree of cross-linking than thermally-cured samples, which was congruent with the FTIR results. Improved or equivalent properties were obtained for VFM-cured samples at shorter cure cycles and lower cure temperatures compared to thermally-cured films. The PNB dielectric was also used as an overcoat material to make micro and nano fluidic channels. In this work, incorporation of advanced micro/nano fluidics with high-sensitivity photonic sensors was demonstrated. 500 nm to 50 µm channels were fabricated by thermal decomposition of epoxy-based PNB polymers. Microdisks with quality factors of over 106 were presented in complementary metal-xide-semiconductor (CMOS) compatible SiN on oxide technology. These ultra-high quality factor SiN resonators were demonstrated in the visible range for the first time. The fluidic structures were interfaced with photonics for index and florescence sensing. This study was a collaboration with Dr. Ehsan Shahhosseini from the Photonics Group at Georgia Tech.

Block copolymers are commercially significant and fundamentally interesting class of polymeric materials. The ability to undergo interfacial thermodynamics-controlled microphase separation from a completely disordered state in the melt to a specifically defined ordered structure through self-organization makes the block copolymers based materials unique. Block copolymer are strongly replacing many of the commercially available polymers due to their unique microstructure and properties. The most practical interests of block copolymers lie in the area of thermoplastic elastomers (TPEs). The objective of the present thesis work is to developing novel roots for enhancing the physical and mechanical properties in block copolymer and multigraft copolymers. Initially the properties are tailored by controlling chemical architecture at synthesis level and by selective blending at production level. This gives an easy access for improvement of the material properties and this is one of my major tasks in the present research modules. Further the block copolymer based TPEs are cross-linked in presence of electron beam (EB) radiation for developing materials with superior properties. The electron beam radiation has the ability to alter material parameters at molecular level for enhancing the macroscopic properties. The desirable physical and chemical properties can be easily attained by varying the radiation beam parameters. In addition to that, controlling the material at nanometer scale is one of the greatest challenges for current nanocomposite research. In elastomeric materials it is very prominent to fill the rubber matrix with nano particles from carbon or silica by melt mixing technique for enhancing the material properties. Other than conventional melt mixing technique, sol–gel processing is also a versatile technique, which making it possible to produce a wide variety of materials and to provide existing materials with novel properties. A combination of in situ sol-gel reaction with electron beam cross-linking in TPEs from triblock copolymer has been demonstrated for the first time as one of the novel nanocomposite system in this work. The main advantage of this system lies in controlling the material behaviour by finely tuning the size of silica nano particle generated inside TPE during in situ sol-gel reaction. Finally, the various roots employed for enhancing the material behaviour in block copolymers in the above research module were secussfully employed on super elastic multigraft copolymers for improving their strength withour sacrificing the super elastic nature.

New processes for the production of polymeric dispersions with high solids content and low viscosity were developed, investigated and characterized. The specifications required for the desired application of paper coating, which constitutes one of the major innovative aspects of this thesis, requires in average particle sizes smaller than 200 nm. This particle size is significantly smaller than obtained in previous work in this area. The main objective of this project was to increase the solids content of existing products from ~50 to ~60 wt% while keeping the viscosity at low levels (< 1200 mPa•s at 20 s-1). In order to produce high solids content latexes with low viscosity, bimodal particle size distributions were resorted to. To obtain highest packing fraction, the small particle size population should be about 7 times smaller than the large particles, bringing the size of the small particles to less than 30 nm. Modified (micro)emulsion processes were developed in order to produce small particle size latex with reduced surfactant concentration and increased solids content. The large particle population was developed using a semi-batch emulsion polymerization process, simulating a product that is commercially available (~52 wt% solids content and viscosity of ~500 mPa•s at 20 s-1). To increase the solids content of this product up to 60 wt%, a second population of small particles was created using two approaches. In the first approach, the small particles were generated in situ using the modified (micro)emulsion approaches developed previously. This process resulted in latexes of ~ 60% solids content and viscosities lower than 500 mPa•s at 20 s-1. In the second approach, the second population of particles was created by the addition of seeds by using small cross-linked particles as pseudo inert-fillers. This process resulted in products with ~58% solids and viscosities lower than 1400 mPa•s at 20 s-1. The slightly decreased solids content and increased viscosity relative to the previous approaches is due to the difficulty in producing cross-linked seeds with particle sizes smaller than 30 nm at an acceptable concentration, causing deviations from ideal conditions. / Thesis (Ph.D, Chemical Engineering) -- Queen's University, 2011-05-03 13:58:44.22

Polyamideamine epichlorohydrin (PAE) resin is a water soluble additive and the most used permanent wet strength additive in alkaline conditions for preparing wet strengthened papers. In this thesis, we studied some properties of PAE resins and wet strengthened papers prepared from them. In order to elucidate PAE structure, liquid state, 1H and 13C NMR was performed and permitted signals assignment of PAE structure. PAE films were prepared to study cross-linking reactions and then thermal and ageing treatments were performed. According to our results, the main PAE cross-linking reaction occurs by a nucleophilic attack of N atoms in the PAE and/or polyamideamine structures forming 2-propanol bridges between PAE macromolecules. A secondary contribution of ester linkages to the PAE cross-linking was also observed. However, this reaction, which is thermally induced, only occurs under anhydrous conditions. The mechanism related to wet strength development of PAE-based papers was studied by using CMC as a model compound for cellulosic fibres and PAE-CMC interactions as a model for PAE-fibres interactions. Based on results from NMR and FTIR, we clearly showed that PAE react with CMC that is when carboxylic groups are present in great amounts. Consequently, as the number of carboxylic groups present in lignocellulosic fibres is considerably less important and the resulting formed ester bonds are hydrolysable, we postulate that ester bond formation has a negligible impact on the wet strength of PAE-based papers. In the second part of this work, a 100% Eucalyptus pulp suspension was used to prepare PAE-based papers. PAE was added at different dosages (0.4, 0.6 and 1%) into the pulp suspension and its adsorption was indirectly followed by measuring the zeta potential. Results indicate that the adsorption, reconformation and/or penetration phenomena reach an apparent equilibrium between 10 and 30 min. Moreover, we showed that the paper dry strength was not significantly affected by the conductivity level (from 100 to 3000 µS/cm) of the pulp suspension. However, the conductivity has an impact on the wet strength and this effect seems to be enhanced for the highest PAE dosage (1%). We also demonstrated that storing the treated paper under controlled conditions or boosting the PAE cross-linking with a thermal post-treatment does not necessarily lead to the same wet strength. Degrading studies of cross-linked PAE films showed that PAE degradation in a persulfate solution at alkaline medium was more effective. A preliminary study of industrial PAE-based papers (coated and uncoated papers) was also performed. For uncoated paper, persulfate treatment was the most efficient. For coated papers, all treatments were inefficient in the used conditions, although a decrease of the wet tensile force of degraded samples was observed. The main responsible of the decrease of persulfate efficiency for coated papers was probably related to side reactions of free radicals with the coating constituents.

We investigated attachment and migration of human retinal pigment epithelial cells (primary, SV40-transfected and ARPE-19) on nanoscopically defined, two-dimensional matrices composed of parallel-aligned collagen type I fibrils. These matrices were used non-cross-linked (native) or after riboflavin/UV-A cross-linking to study cell attachment and migration by time-lapse video microscopy. Expression of collagen type I and IV, MMP-2 and of the collagen-binding integrin subunit α2 were examined by immunofluorescence and Western blotting. SV40-RPE cells quickly attached to the nanostructured collagen matrices and aligned along the collagen fibrils. However, they disrupted both native and cross-linked collagen matrices within 5 h. Primary RPE cells aligned more slowly without destroying either native or cross-linked substrates. Compared to primary RPE cells, ARPE-19 cells showed reduced alignment but partially disrupted the matrices within 20 h after seeding. Expression of the collagen type I-binding integrin subunit α2 was highest in SV40-RPE cells, lower in primary RPE cells and almost undetectable in ARPE-19 cells. Thus, integrin α2 expression levels directly correlated with the degree of cell alignment in all examined RPE cell types. Specific integrin subunit α2-mediated matrix binding was verified by preincubation with an α2-function-blocking antibody, which impaired cell adhesion and alignment to varying degrees in primary and SV40-RPE cells. Since native matrices supported extended and directed primary RPE cell growth, optimizing the matrix production procedure may in the future yield nanostructured collagen matrices serving as transferable cell sheet carriers. / Dieser Beitrag ist mit Zustimmung des Rechteinhabers aufgrund einer (DFG-geförderten) Allianz- bzw. Nationallizenz frei zugänglich.

Rupture of the anterior cruciate ligament (ACL) of the knee leads to chronic joint instability and reduced range of motion while the long term results are marred by a high prevalence of degenerative joint disease especially osteoarthritis. Bundles of collagen threads have been widely investigated for the repair of torn ACL, but are limited by insufficient tissue ingrowth to repopulate and completely regenerate these grafts. We have developed a novel in vitro method of characterizing fiber-based thread matrices by probing their ability to promote tissue ingrowth from a wound margin as a measure of their ability to promote repopulation and regeneration. This method is useful in the optimization of thread scaffolds, and is sensitive enough to distinguish between subtle variations in biopolymer chemistry and organization. Furthermore, this method was used to characterize the effects of crosslinking on the cell outgrowth and correlated the findings with the mechanical properties of collagen threads. The results suggest that crosslinking is required to achieve sufficient mechanical properties for high stress applications such as ACL replacement, but regardless of technique, crosslinking attenuated the cell outgrowth properties of the threads. To improve the regenerative capacity of these scaffolds, novel fibrin microthread matrices were developed with a similar morphology to collagen threads and sufficient mechanical strength to be incorporated in composite thread scaffold systems. These fibrin microthreads were loaded with FGF-2, a potent mitogen and chemotactic agent that works synergistically with fibrin in regulating cell signaling and gene expression. Increases in fibroblast migration and proliferation in FGF-2-loaded fibrin threads were successfully demonstrated with the concomitant promotion of oriented, aligned, spindle-like fibroblast morphology. These results suggest that fibrin-FGF-2 microthreads have distinct advantages as a biomaterial for the rapid regeneration of injured tissues such as the ACL.

Submitted by JULIANA ROSA LUIZ ALONSO null (ju29alonso@hotmail.com) on 2016-05-02T19:21:59Z No. of bitstreams: 1 Versão Final_Dissertação_Juliana Alonso.pdf: 3284684 bytes, checksum: 5cf89df8ddd554ca35ba036626ed5bdb (MD5) / Approved for entry into archive by Felipe Augusto Arakaki (arakaki@reitoria.unesp.br) on 2016-05-04T18:51:25Z (GMT) No. of bitstreams: 1 alonso_jrl_me_arafo.pdf: 3284684 bytes, checksum: 5cf89df8ddd554ca35ba036626ed5bdb (MD5) / Made available in DSpace on 2016-05-04T18:51:25Z (GMT). No. of bitstreams: 1 alonso_jrl_me_arafo.pdf: 3284684 bytes, checksum: 5cf89df8ddd554ca35ba036626ed5bdb (MD5) Previous issue date: 2016-04-06 / Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP) / A estabilidade da união resina-dentina pode ser melhorada pelo uso de agentes promotores de ligações cruzadas (cross-linkers). Todavia, existe pouca informação quanto ao desempenho desses agentes em dentina radicular. Portanto, o objetivo do presente estudo foi avaliar o efeito de três cross-linkers na atividade proteolítica e na resistência da união cimento resinoso-dentina radicular. Raízes unirradiculares foram obtidas de pré-molares humanos (n=48). Após tratamento endodôntico, essas raízes foram distribuídas em 4 grupos (n=12): água deionizada (controle), carbodiimida (EDC) 0,5 mol/L, proantocianidina (PA) 5% ou glutaraldeído (GD) 5%. Decorridas 24h do tratamento com esses agentes e da cimentação de pinos de fibra de vidro com cimento resinoso, as raízes foram seccionadas transversalmente para a obtenção de espécimes com 1 mm de espessura, das regiões cervical, média e apical. Nove raízes por grupo foram utilizadas para o ensaio mecânico de extrusão e três para determinação da atividade proteolítica dentinária, por meio de zimografia in situ. Os dados de resistência de união (RU) foram submetidos aos testes de ANOVA e Tukey e a existência de associação entre o tipo de fratura e as variáveis independentes do estudo foi determinada pelo teste de qui-quadrado (2) (=0,05). Nenhum dos cross-linkers afetou a RU imediata. GD aumentou esses valores significativamente em comparação à PA, mas não ao controle. Houve redução significante da RU do terço cervical para o apical, exceto para o grupo PA. Aumento na porcentagem de fraturas adesivas entre o pino de fibra de vidro e o cimento resinoso foi observado para os grupos EDC e GD, em relação ao grupo controle, enquanto, para PA, houve aumento de fraturas adesivas entre o cimento resinoso e a dentina. Foi observada grande atividade gelatinolítica no grupo controle, a qual foi reduzida por todos os cross-linkers . Em conclusão, além de não interferirem negativamente na RU imediata, os cross-linkers reduziram a atividade proteolítica na camada híbrida da união cimento resinoso-dentina radicular. / The resin-dentin bond stability can be improved by the use of cross-linkers. However, only scarce information is available as to the performance of these agents on root dentin. Therefore, the aim of this study was to evaluate the effect of three cross-linkers on the proteolytic activity of root dentin and on the bond strength of resin-based cement-root dentin interfaces. Single canal roots were obtained from human premolars (n=48). After endodontic treatment, they were randomly divided into four groups: deionized water (control), 0.5 mol/L carbodiimide (EDC), 5% proanthocyanidin (PA) or 5% glutaraldehyde (GD). After 24h from dentin treatment with the cross-linkers and the cementation of a fiber post with a resin-based cement, the roots were transversally sectioned to obtain 1 mm-thick specimens, from the cervical, mid and apical areas. Nine roots per group were used for the push-out test and three for determining the proteolytic activity of the root dentin by in situ zymography. Bond strength data were submitted to ANOVA and Tukey tests and the existence of an association between the type of fracture and the independent variables of the study was determined by chi-square test (=0.05). None of the cross-linkers affected the bond strength. GD increased bond strength compared to PA, but both were similar to the control. Significant reduction in bond strength was observed between the cervical and the apical root thirds. Increase in the percentage of adhesive fractures between the glass fiber post and resin cement was observed for EDC and GD groups, in comparison with the control group, while for PA, an increase of adhesive fractures between the resin cement and dentin was observed. Intense gelatinolytic activity was seen in the control group which was remarkably reduced in the cross-linker-treated groups. In conclusion, besides not interfering with bond strength, the cross-linkers reduced the proteolytic activity in the hybrid layers of the resin cement-root dentin bond. / FAPESP: 2014/10183-8